Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Parallax Medical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 12, 2003: TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TA.
| Dec 12, 2003 | TRACERS TA BONE CEMENT OPACIFIER, MODEL TCR-TAK033230 · MYU | 510(k) clearances |
| Mar 11, 2003 | TRACERS BONE CEMENT OPACIFIERK023445 · MYU | 510(k) clearances |
| Jul 25, 2002 | CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLESK022169 · KNW | 510(k) clearances |
| Jul 18, 2001 | PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLESK011206 · KNW | 510(k) clearances |
| Aug 31, 2000 | PARALLAX CRANIOSETK994022 · GXP | 510(k) clearances |
| Aug 13, 1999 | PARALLAX TRACER RADIOPAQUE PARTICLESK991893 · MYU | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
